Canonical Allele Identifier: CA380468887
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1554982166
MyVariant Identifiers: chr11:g.55579071del (hg19) chr11:g.55811596del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811597del , CM000673.2:g.55811597del GRCh38
NC_000011.9:g.55579073del , CM000673.1:g.55579073del GRCh37
NC_000011.8:g.55335649del NCBI36
NG_052620.1:g.5231del

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.131del MANE Select ENSP00000485319.1:p.Gly44AlafsTer2
ENST00000333973.3:c.131del ENSP00000335529.2:p.Gly44AlafsTer2
ENST00000623450.1:c.131del ENSP00000485509.1:p.Gly44AlafsTer2
ENST00000625203.1:c.131del ENSP00000485319.1:p.Gly44AlafsTer2
NM_001004738.1:c.131del NP_001004738.1:p.Gly44AlafsTer2
NM_001004738.2:c.131del MANE Select NP_001004738.1:p.Gly44AlafsTer2
Search 100 bp 5'
Search 100 bp 3'